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Innovative thinking of clinical investigation for rare disease drug development

For the development of a test treatment or drug product, it is necessary to conduct composite hypothesis testing to test for effectiveness and safety simultaneously, since some approved drug products have been recalled due to safety concerns. One of the major issues in conducting a composite hypothe...

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Autores principales: Wang, Peijin, Chow, Shein-Chung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10517458/
https://www.ncbi.nlm.nih.gov/pubmed/37740206
http://dx.doi.org/10.1186/s13023-023-02909-w
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author Wang, Peijin
Chow, Shein-Chung
author_facet Wang, Peijin
Chow, Shein-Chung
author_sort Wang, Peijin
collection PubMed
description For the development of a test treatment or drug product, it is necessary to conduct composite hypothesis testing to test for effectiveness and safety simultaneously, since some approved drug products have been recalled due to safety concerns. One of the major issues in conducting a composite hypothesis testing for effectiveness and safety is the requirement of a huge sample size to achieve the desired power for detecting clinically meaningful differences in both safety and effectiveness. Situation can be much difficult in orphan drug development. In this article, a generalized two-stage innovative approach to test for effectiveness and safety simultaneously is proposed. Additionally, to alleviate the requirement of a large randomized clinical trial (RCT) and revealing effectiveness, real-world data is suggested to use in conjunction with RCT data for orphan drug development. The proposed approach can help investigators test for effectiveness and safety at the same time without worrying about the sample size. It also helps reduce the probability of approving a drug product with safety concerns.
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spelling pubmed-105174582023-09-24 Innovative thinking of clinical investigation for rare disease drug development Wang, Peijin Chow, Shein-Chung Orphanet J Rare Dis Review For the development of a test treatment or drug product, it is necessary to conduct composite hypothesis testing to test for effectiveness and safety simultaneously, since some approved drug products have been recalled due to safety concerns. One of the major issues in conducting a composite hypothesis testing for effectiveness and safety is the requirement of a huge sample size to achieve the desired power for detecting clinically meaningful differences in both safety and effectiveness. Situation can be much difficult in orphan drug development. In this article, a generalized two-stage innovative approach to test for effectiveness and safety simultaneously is proposed. Additionally, to alleviate the requirement of a large randomized clinical trial (RCT) and revealing effectiveness, real-world data is suggested to use in conjunction with RCT data for orphan drug development. The proposed approach can help investigators test for effectiveness and safety at the same time without worrying about the sample size. It also helps reduce the probability of approving a drug product with safety concerns. BioMed Central 2023-09-22 /pmc/articles/PMC10517458/ /pubmed/37740206 http://dx.doi.org/10.1186/s13023-023-02909-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Wang, Peijin
Chow, Shein-Chung
Innovative thinking of clinical investigation for rare disease drug development
title Innovative thinking of clinical investigation for rare disease drug development
title_full Innovative thinking of clinical investigation for rare disease drug development
title_fullStr Innovative thinking of clinical investigation for rare disease drug development
title_full_unstemmed Innovative thinking of clinical investigation for rare disease drug development
title_short Innovative thinking of clinical investigation for rare disease drug development
title_sort innovative thinking of clinical investigation for rare disease drug development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10517458/
https://www.ncbi.nlm.nih.gov/pubmed/37740206
http://dx.doi.org/10.1186/s13023-023-02909-w
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